These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

122 related articles for article (PubMed ID: 10407849)

  • 1. Behavioral characterization of mdx3cv mice deficient in C-terminal dystrophins.
    Vaillend C; Ungerer A
    Neuromuscul Disord; 1999 Jul; 9(5):296-304. PubMed ID: 10407849
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Spatial discrimination learning and CA1 hippocampal synaptic plasticity in mdx and mdx3cv mice lacking dystrophin gene products.
    Vaillend C; Billard JM; Claudepierre T; Rendon A; Dutar P; Ungerer A
    Neuroscience; 1998 Sep; 86(1):53-66. PubMed ID: 9692743
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Influence of dystrophin-gene mutation on mdx mouse behavior. I. Retention deficits at long delays in spontaneous alternation and bar-pressing tasks.
    Vaillend C; Rendon A; Misslin R; Ungerer A
    Behav Genet; 1995 Nov; 25(6):569-79. PubMed ID: 8540895
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Characterization of brain dystrophins absence and impact in dystrophin-deficient Dmdmdx rat model.
    Caudal D; François V; Lafoux A; Ledevin M; Anegon I; Le Guiner C; Larcher T; Huchet C
    PLoS One; 2020; 15(3):e0230083. PubMed ID: 32160266
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Cognitive dysfunction in the dystrophin-deficient mouse model of Duchenne muscular dystrophy: A reappraisal from sensory to executive processes.
    Chaussenot R; Edeline JM; Le Bec B; El Massioui N; Laroche S; Vaillend C
    Neurobiol Learn Mem; 2015 Oct; 124():111-22. PubMed ID: 26190833
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Muscular dystrophy in mice caused by two different alterations of dystrophin gene.
    Rowiński J; Kozłowska H; Sulikowska-Rowińska A; Rejment E
    Folia Histochem Cytobiol; 2001; 39(2):119-20. PubMed ID: 11374785
    [TBL] [Abstract][Full Text] [Related]  

  • 7. DMD(mdx3Cv) and DMD(mdx4Cv) dystrophin mutations in mice: rapid polymerase chain reaction genotyping.
    Pearson-White SH
    Neuromuscul Disord; 2002 May; 12(4):366-70. PubMed ID: 12062254
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hypoxia on hippocampal slices from mice deficient in dystrophin (mdx) and isoforms (mdx3cv).
    Godfraind JM; Tekkök SB; Krnjević K
    J Cereb Blood Flow Metab; 2000 Jan; 20(1):145-52. PubMed ID: 10616803
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Testing of SHIRPA, a mouse phenotypic assessment protocol, on Dmd(mdx) and Dmd(mdx3cv) dystrophin-deficient mice.
    Rafael JA; Nitta Y; Peters J; Davies KE
    Mamm Genome; 2000 Sep; 11(9):725-8. PubMed ID: 10967129
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cognitive flexibility deficits in a mouse model for the absence of full-length dystrophin.
    Remmelink E; Aartsma-Rus A; Smit AB; Verhage M; Loos M; van Putten M
    Genes Brain Behav; 2016 Jul; 15(6):558-67. PubMed ID: 27220066
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Impaired long-term spatial and recognition memory and enhanced CA1 hippocampal LTP in the dystrophin-deficient Dmd(mdx) mouse.
    Vaillend C; Billard JM; Laroche S
    Neurobiol Dis; 2004 Oct; 17(1):10-20. PubMed ID: 15350961
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Effects of dystrophin isoforms on signal transduction through neural retina: genotype-phenotype analysis of duchenne muscular dystrophy mouse mutants.
    Pillers DA; Weleber RG; Green DG; Rash SM; Dally GY; Howard PL; Powers MR; Hood DC; Chapman VM; Ray PN; Woodward WR
    Mol Genet Metab; 1999 Feb; 66(2):100-10. PubMed ID: 10068512
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Learning, memory and blood-brain barrier pathology in Duchenne muscular dystrophy mice lacking Dp427, or Dp427 and Dp140.
    Verhaeg M; Adamzek K; van de Vijver D; Putker K; Engelbeen S; Wijnbergen D; Overzier M; Suidgeest E; van der Weerd L; Aartsma-Rus A; van Putten M
    Genes Brain Behav; 2024 Jun; 23(3):e12895. PubMed ID: 38837620
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Social and emotional alterations in mice lacking the short dystrophin-gene product, Dp71.
    Miranda R; Ceschi L; Le Verger D; Nagapin F; Edeline JM; Chaussenot R; Vaillend C
    Behav Brain Funct; 2024 Aug; 20(1):21. PubMed ID: 39182120
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Upregulation of brain utrophin does not rescue behavioral alterations in dystrophin-deficient mice.
    Perronnet C; Chagneau C; Le Blanc P; Samson-Desvignes N; Mornet D; Laroche S; De La Porte S; Vaillend C
    Hum Mol Genet; 2012 May; 21(10):2263-76. PubMed ID: 22343141
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Subcellular localization of dystrophin isoforms in cardiomyocytes and phenotypic analysis of dystrophin-deficient mice reveal cardiac myopathy is predominantly caused by a deficiency in full-length dystrophin.
    Masubuchi N; Shidoh Y; Kondo S; Takatoh J; Hanaoka K
    Exp Anim; 2013; 62(3):211-7. PubMed ID: 23903056
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Normal cochlear function in mdx and mdx(Cv3) Duchenne muscular dystrophy mouse models.
    Pillers DA; Duncan NM; Dwinnell SJ; Rash SM; Kempton JB; Trune DR
    Laryngoscope; 1999 Aug; 109(8):1310-2. PubMed ID: 10443839
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Smooth muscle-specific dystrophin expression improves aberrant vasoregulation in mdx mice.
    Ito K; Kimura S; Ozasa S; Matsukura M; Ikezawa M; Yoshioka K; Ueno H; Suzuki M; Araki K; Yamamura K; Miwa T; Dickson G; Thomas GD; Miike T
    Hum Mol Genet; 2006 Jul; 15(14):2266-75. PubMed ID: 16777842
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The frequency of revertants in mdx mouse genetic models for Duchenne muscular dystrophy.
    Danko I; Chapman V; Wolff JA
    Pediatr Res; 1992 Jul; 32(1):128-31. PubMed ID: 1635838
    [TBL] [Abstract][Full Text] [Related]  

  • 20. New mdx mutation disrupts expression of muscle and nonmuscle isoforms of dystrophin.
    Cox GA; Phelps SF; Chapman VM; Chamberlain JS
    Nat Genet; 1993 May; 4(1):87-93. PubMed ID: 8099842
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.